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Data last updated: Apr 2025
Patient Transfer Sheet
3661908L030-704R
On Market
Class I
Regulation
EU MDR
Manufacturer
Segetex-eif
Primary DI
03661908009532
Reference
L030-70
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Identification
Primary DI
03661908009532
Basic UDI-DI
3661908L030-704R
Reference
L030-70
Issuing Agency
—
ULID
YY1HN3Z5
Classification
Risk Class
Class I
Regulation
EU MDR
Status
On Market
Device Types
Coming soon
Manufacturer
Manufacturer
Segetex-eif
Manufacturer SRN
FR-MF-000007669
Manufacturer Status
Active
CND Nomenclature
V0599
CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER
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